Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 38524015 | Congenital erythropoietic porphyria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 38525019 | Gunther's disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 38526018 | Congenital photosensitive porphyria | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 38527010 | Congenital porphyria | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 38528017 | Hematoporphyria congenita | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 38529013 | Porphyria erythropoietica | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 481477016 | Haematoporphyria congenita | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 752399013 | Congenital erythropoietic porphyria (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 1223000017 | Uroporphyrinogen III synthase deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 1223001018 | CEP - Congenital erythropoietic porphyria | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital erythropoietic porphyria | Is a | Erythropoietic porphyria | true | Inferred relationship | Existential restriction modifier | ||
| Congenital erythropoietic porphyria | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital erythropoietic porphyria | Finding site | Body system structure | false | Inferred relationship | Existential restriction modifier | ||
| Congenital erythropoietic porphyria | Is a | Congenital porphyria | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR